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Trazodone Hydrochloride

NDC 80425-0462 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAdvanced Rx of Tennessee, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA202180
Dosage form / routeTABLET · ORAL
Active ingredientsTRAZODONE HYDROCHLORIDE (150 mg/1)
Marketing started20241219
Package count3

External sources

Source: openFDA. Public-domain (CC0).